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Th17 cells require the DNA repair sensor xeroderma pigmentosum complementation Group C to control oxidative DNA damage in a murine model
Abstract T helper 17 cells play essential roles in mucosal immunity and autoimmunity, yet the mechanisms that protect these cells from oxidative DNA damage remain poorly defined. Here we show, in a murine model, that the nucleotide excision repair sensor Xeroderma Pigmentosum Complementation Group C preserves genomic stability and metabolic fitness during T helper 17 cell differentiation.
Genomic epidemiology of SARS-CoV-2 in large university hospital cohort: the UnCoVER-Brazil project | Epidemiology & Infection | Cambridge Core
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus that causes coronavirus disease (COVID-19), remains a global threat despite massive diagnostic testing, isolation, therapies, and vaccines. Emerging SARS-CoV-2 variants of concern (VOCs) continue to challenge these measures with increased transmissibility or virulence, escape of host antibody neutralization, and decreased efficacy of detection, therapeutics, and vaccination [Reference Aleem, Akbar Samad and Slenker1].
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